Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
T |
C |
1: 179,580,946 (GRCm39) |
E1752G |
possibly damaging |
Het |
Aqp3 |
T |
C |
4: 41,095,178 (GRCm39) |
T68A |
probably damaging |
Het |
Arhgap40 |
A |
G |
2: 158,385,147 (GRCm39) |
K463R |
probably damaging |
Het |
Asb10 |
A |
T |
5: 24,738,736 (GRCm39) |
C440* |
probably null |
Het |
Bach1 |
A |
G |
16: 87,526,385 (GRCm39) |
T616A |
probably damaging |
Het |
Braf |
T |
A |
6: 39,642,042 (GRCm39) |
|
probably null |
Het |
Cacna1s |
A |
T |
1: 136,020,371 (GRCm39) |
N803Y |
probably damaging |
Het |
Cald1 |
A |
G |
6: 34,663,000 (GRCm39) |
E21G |
probably damaging |
Het |
Caskin1 |
G |
T |
17: 24,722,898 (GRCm39) |
G589C |
probably damaging |
Het |
Cdc37l1 |
T |
C |
19: 28,968,071 (GRCm39) |
|
probably null |
Het |
Cntnap5b |
G |
A |
1: 100,306,815 (GRCm39) |
G844D |
probably damaging |
Het |
Col5a1 |
T |
C |
2: 27,914,762 (GRCm39) |
L1615P |
unknown |
Het |
Cpt1a |
C |
A |
19: 3,430,155 (GRCm39) |
P672T |
probably damaging |
Het |
Defb22 |
A |
G |
2: 152,328,117 (GRCm39) |
Y23H |
probably damaging |
Het |
Depdc1b |
G |
C |
13: 108,500,166 (GRCm39) |
K226N |
probably damaging |
Het |
Derl2 |
A |
G |
11: 70,909,764 (GRCm39) |
|
probably benign |
Het |
Dnaja2 |
T |
C |
8: 86,265,982 (GRCm39) |
T368A |
probably benign |
Het |
Dsg3 |
C |
A |
18: 20,673,254 (GRCm39) |
T975K |
possibly damaging |
Het |
Eif4enif1 |
T |
A |
11: 3,170,269 (GRCm39) |
D107E |
probably damaging |
Het |
Fut11 |
A |
G |
14: 20,746,325 (GRCm39) |
D389G |
probably damaging |
Het |
Gopc |
C |
T |
10: 52,225,328 (GRCm39) |
G299E |
probably damaging |
Het |
Gprin1 |
T |
C |
13: 54,886,423 (GRCm39) |
D617G |
probably benign |
Het |
Grin2d |
A |
G |
7: 45,506,960 (GRCm39) |
V505A |
probably damaging |
Het |
Heatr6 |
T |
C |
11: 83,650,161 (GRCm39) |
Y206H |
probably damaging |
Het |
Hhex |
C |
A |
19: 37,425,713 (GRCm39) |
N147K |
probably damaging |
Het |
Igkv4-80 |
G |
A |
6: 68,993,699 (GRCm39) |
S64F |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,625,068 (GRCm39) |
K360R |
possibly damaging |
Het |
Kat5 |
AG |
A |
19: 5,658,297 (GRCm39) |
|
probably null |
Het |
Kat5 |
T |
A |
19: 5,658,302 (GRCm39) |
N191I |
probably benign |
Het |
Kifc5b |
A |
G |
17: 27,144,597 (GRCm39) |
D572G |
probably damaging |
Het |
Lrp5 |
C |
A |
19: 3,662,197 (GRCm39) |
|
probably null |
Het |
Lrtm1 |
A |
G |
14: 28,749,673 (GRCm39) |
M345V |
probably benign |
Het |
Mbd5 |
T |
C |
2: 49,162,461 (GRCm39) |
V981A |
probably benign |
Het |
Mier3 |
G |
A |
13: 111,841,783 (GRCm39) |
G115S |
possibly damaging |
Het |
Mrgprd |
A |
G |
7: 144,875,261 (GRCm39) |
N44S |
probably damaging |
Het |
Mrps10 |
C |
A |
17: 47,689,146 (GRCm39) |
P181Q |
probably damaging |
Het |
Myot |
T |
A |
18: 44,470,075 (GRCm39) |
C17* |
probably null |
Het |
Myt1 |
A |
G |
2: 181,409,498 (GRCm39) |
|
probably null |
Het |
Or4d11 |
T |
C |
19: 12,013,363 (GRCm39) |
T248A |
probably benign |
Het |
Or4d6 |
T |
C |
19: 12,086,061 (GRCm39) |
N57S |
probably damaging |
Het |
Or4e5 |
T |
C |
14: 52,727,638 (GRCm39) |
Y261C |
probably damaging |
Het |
Or7a39 |
C |
A |
10: 78,715,288 (GRCm39) |
T94K |
probably damaging |
Het |
Or7e165 |
T |
A |
9: 19,694,507 (GRCm39) |
I26N |
possibly damaging |
Het |
Osbpl6 |
G |
A |
2: 76,379,794 (GRCm39) |
G128E |
probably damaging |
Het |
P3h3 |
A |
T |
6: 124,832,233 (GRCm39) |
Y218N |
probably damaging |
Het |
Paxip1 |
A |
G |
5: 27,986,418 (GRCm39) |
|
probably null |
Het |
Pdia5 |
T |
C |
16: 35,250,284 (GRCm39) |
Y225C |
probably damaging |
Het |
Pik3c2g |
T |
G |
6: 139,801,079 (GRCm39) |
M526R |
|
Het |
Prox1 |
A |
G |
1: 189,894,323 (GRCm39) |
F41L |
probably benign |
Het |
Psd3 |
A |
T |
8: 68,453,408 (GRCm39) |
F284I |
probably damaging |
Het |
Rev3l |
T |
A |
10: 39,699,678 (GRCm39) |
C1392S |
probably benign |
Het |
Rfxank |
A |
T |
8: 70,587,285 (GRCm39) |
V212E |
probably damaging |
Het |
Ros1 |
T |
C |
10: 52,031,222 (GRCm39) |
D482G |
probably benign |
Het |
Sat2 |
A |
T |
11: 69,513,763 (GRCm39) |
I94F |
probably damaging |
Het |
Scarf2 |
T |
C |
16: 17,621,702 (GRCm39) |
L384P |
probably damaging |
Het |
Sec14l2 |
C |
A |
11: 4,066,750 (GRCm39) |
E21* |
probably null |
Het |
Slitrk5 |
T |
A |
14: 111,918,131 (GRCm39) |
V585E |
probably benign |
Het |
Spata31h1 |
T |
A |
10: 82,123,571 (GRCm39) |
E3146D |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,123,729 (GRCm39) |
S3094G |
probably benign |
Het |
Tas2r130 |
T |
A |
6: 131,607,226 (GRCm39) |
M190L |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,341,597 (GRCm39) |
S1061N |
possibly damaging |
Het |
Tlr9 |
C |
A |
9: 106,102,463 (GRCm39) |
H585N |
probably damaging |
Het |
Tmem219 |
A |
T |
7: 126,495,947 (GRCm39) |
I142N |
probably damaging |
Het |
Tnni2 |
A |
G |
7: 141,996,915 (GRCm39) |
N8S |
probably benign |
Het |
Tnpo2 |
G |
A |
8: 85,776,748 (GRCm39) |
R485H |
probably damaging |
Het |
Ttc8 |
A |
G |
12: 98,908,547 (GRCm39) |
E72G |
possibly damaging |
Het |
Upf1 |
A |
G |
8: 70,793,268 (GRCm39) |
Y297H |
probably damaging |
Het |
Vmn1r4 |
A |
G |
6: 56,933,721 (GRCm39) |
K75R |
probably damaging |
Het |
Vmn2r78 |
G |
A |
7: 86,571,633 (GRCm39) |
G481D |
probably benign |
Het |
Vmn2r96 |
A |
G |
17: 18,803,302 (GRCm39) |
Y404C |
probably damaging |
Het |
Vps50 |
T |
A |
6: 3,602,708 (GRCm39) |
S942T |
probably benign |
Het |
Xkr7 |
C |
A |
2: 152,895,983 (GRCm39) |
S279* |
probably null |
Het |
Zan |
G |
A |
5: 137,432,416 (GRCm39) |
Q2294* |
probably null |
Het |
Zan |
T |
C |
5: 137,448,753 (GRCm39) |
Y1700C |
unknown |
Het |
|
Other mutations in Ncoa6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Ncoa6
|
APN |
2 |
155,248,128 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00849:Ncoa6
|
APN |
2 |
155,263,608 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00933:Ncoa6
|
APN |
2 |
155,257,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00981:Ncoa6
|
APN |
2 |
155,248,099 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01420:Ncoa6
|
APN |
2 |
155,249,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Ncoa6
|
APN |
2 |
155,263,003 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03049:Ncoa6
|
APN |
2 |
155,260,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03194:Ncoa6
|
APN |
2 |
155,257,788 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03269:Ncoa6
|
APN |
2 |
155,248,409 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03299:Ncoa6
|
APN |
2 |
155,249,207 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03306:Ncoa6
|
APN |
2 |
155,247,427 (GRCm39) |
missense |
probably benign |
0.30 |
alcoa
|
UTSW |
2 |
155,244,584 (GRCm39) |
unclassified |
probably benign |
|
Aluminum
|
UTSW |
2 |
155,241,613 (GRCm39) |
critical splice acceptor site |
probably null |
|
balboa
|
UTSW |
2 |
155,248,869 (GRCm39) |
missense |
probably benign |
0.05 |
mauna_loa
|
UTSW |
2 |
155,257,147 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4466001:Ncoa6
|
UTSW |
2 |
155,247,577 (GRCm39) |
missense |
probably benign |
|
R0011:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0014:Ncoa6
|
UTSW |
2 |
155,279,963 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0079:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0080:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0081:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0164:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0166:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0172:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0173:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0245:Ncoa6
|
UTSW |
2 |
155,233,131 (GRCm39) |
missense |
probably benign |
0.00 |
R0284:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0285:Ncoa6
|
UTSW |
2 |
155,257,621 (GRCm39) |
missense |
probably damaging |
0.96 |
R0285:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0288:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0539:Ncoa6
|
UTSW |
2 |
155,257,617 (GRCm39) |
missense |
probably benign |
0.08 |
R0652:Ncoa6
|
UTSW |
2 |
155,233,131 (GRCm39) |
missense |
probably benign |
0.00 |
R0781:Ncoa6
|
UTSW |
2 |
155,253,440 (GRCm39) |
splice site |
probably benign |
|
R1053:Ncoa6
|
UTSW |
2 |
155,275,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Ncoa6
|
UTSW |
2 |
155,253,440 (GRCm39) |
splice site |
probably benign |
|
R1420:Ncoa6
|
UTSW |
2 |
155,263,073 (GRCm39) |
nonsense |
probably null |
|
R1521:Ncoa6
|
UTSW |
2 |
155,257,142 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1541:Ncoa6
|
UTSW |
2 |
155,257,224 (GRCm39) |
missense |
probably benign |
0.35 |
R1677:Ncoa6
|
UTSW |
2 |
155,244,584 (GRCm39) |
unclassified |
probably benign |
|
R1858:Ncoa6
|
UTSW |
2 |
155,263,559 (GRCm39) |
missense |
probably benign |
0.13 |
R1954:Ncoa6
|
UTSW |
2 |
155,248,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1955:Ncoa6
|
UTSW |
2 |
155,248,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2040:Ncoa6
|
UTSW |
2 |
155,248,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R2087:Ncoa6
|
UTSW |
2 |
155,248,079 (GRCm39) |
nonsense |
probably null |
|
R2159:Ncoa6
|
UTSW |
2 |
155,249,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R2278:Ncoa6
|
UTSW |
2 |
155,249,570 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2696:Ncoa6
|
UTSW |
2 |
155,279,935 (GRCm39) |
missense |
probably benign |
0.45 |
R2891:Ncoa6
|
UTSW |
2 |
155,279,881 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3618:Ncoa6
|
UTSW |
2 |
155,249,709 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3747:Ncoa6
|
UTSW |
2 |
155,253,561 (GRCm39) |
missense |
probably benign |
0.01 |
R3778:Ncoa6
|
UTSW |
2 |
155,263,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Ncoa6
|
UTSW |
2 |
155,249,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R3802:Ncoa6
|
UTSW |
2 |
155,247,484 (GRCm39) |
missense |
probably benign |
|
R3820:Ncoa6
|
UTSW |
2 |
155,248,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R3821:Ncoa6
|
UTSW |
2 |
155,248,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R3822:Ncoa6
|
UTSW |
2 |
155,248,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R3870:Ncoa6
|
UTSW |
2 |
155,257,477 (GRCm39) |
splice site |
probably null |
|
R4037:Ncoa6
|
UTSW |
2 |
155,249,290 (GRCm39) |
missense |
probably damaging |
0.98 |
R4488:Ncoa6
|
UTSW |
2 |
155,249,396 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4719:Ncoa6
|
UTSW |
2 |
155,233,081 (GRCm39) |
unclassified |
probably benign |
|
R4732:Ncoa6
|
UTSW |
2 |
155,263,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Ncoa6
|
UTSW |
2 |
155,263,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Ncoa6
|
UTSW |
2 |
155,257,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R4835:Ncoa6
|
UTSW |
2 |
155,249,053 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4883:Ncoa6
|
UTSW |
2 |
155,248,687 (GRCm39) |
missense |
probably benign |
0.29 |
R4967:Ncoa6
|
UTSW |
2 |
155,263,252 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5021:Ncoa6
|
UTSW |
2 |
155,248,869 (GRCm39) |
missense |
probably benign |
0.05 |
R5234:Ncoa6
|
UTSW |
2 |
155,279,933 (GRCm39) |
missense |
probably benign |
0.01 |
R5356:Ncoa6
|
UTSW |
2 |
155,263,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R5358:Ncoa6
|
UTSW |
2 |
155,248,907 (GRCm39) |
missense |
probably damaging |
0.97 |
R5375:Ncoa6
|
UTSW |
2 |
155,275,915 (GRCm39) |
missense |
probably benign |
0.16 |
R5412:Ncoa6
|
UTSW |
2 |
155,249,701 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5579:Ncoa6
|
UTSW |
2 |
155,248,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R5618:Ncoa6
|
UTSW |
2 |
155,279,817 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5641:Ncoa6
|
UTSW |
2 |
155,263,756 (GRCm39) |
missense |
probably benign |
0.22 |
R5757:Ncoa6
|
UTSW |
2 |
155,253,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R5761:Ncoa6
|
UTSW |
2 |
155,250,061 (GRCm39) |
missense |
probably benign |
0.11 |
R5778:Ncoa6
|
UTSW |
2 |
155,248,688 (GRCm39) |
missense |
probably benign |
0.01 |
R5852:Ncoa6
|
UTSW |
2 |
155,247,419 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5940:Ncoa6
|
UTSW |
2 |
155,257,785 (GRCm39) |
missense |
probably damaging |
0.98 |
R6155:Ncoa6
|
UTSW |
2 |
155,249,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R6374:Ncoa6
|
UTSW |
2 |
155,263,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R6389:Ncoa6
|
UTSW |
2 |
155,237,736 (GRCm39) |
missense |
probably damaging |
0.98 |
R6669:Ncoa6
|
UTSW |
2 |
155,241,613 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7097:Ncoa6
|
UTSW |
2 |
155,279,983 (GRCm39) |
missense |
probably benign |
0.01 |
R7963:Ncoa6
|
UTSW |
2 |
155,247,916 (GRCm39) |
missense |
probably benign |
0.30 |
R8356:Ncoa6
|
UTSW |
2 |
155,248,172 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8698:Ncoa6
|
UTSW |
2 |
155,257,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8859:Ncoa6
|
UTSW |
2 |
155,248,388 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8870:Ncoa6
|
UTSW |
2 |
155,263,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R9041:Ncoa6
|
UTSW |
2 |
155,257,450 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9062:Ncoa6
|
UTSW |
2 |
155,263,348 (GRCm39) |
missense |
probably benign |
0.42 |
R9088:Ncoa6
|
UTSW |
2 |
155,249,726 (GRCm39) |
missense |
probably damaging |
0.98 |
R9225:Ncoa6
|
UTSW |
2 |
155,249,441 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9445:Ncoa6
|
UTSW |
2 |
155,250,063 (GRCm39) |
missense |
probably benign |
0.01 |
R9497:Ncoa6
|
UTSW |
2 |
155,248,238 (GRCm39) |
missense |
probably damaging |
0.97 |
R9514:Ncoa6
|
UTSW |
2 |
155,248,133 (GRCm39) |
missense |
probably benign |
0.19 |
R9656:Ncoa6
|
UTSW |
2 |
155,274,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R9720:Ncoa6
|
UTSW |
2 |
155,250,304 (GRCm39) |
missense |
probably damaging |
0.98 |
R9732:Ncoa6
|
UTSW |
2 |
155,244,636 (GRCm39) |
missense |
probably damaging |
0.99 |
RF033:Ncoa6
|
UTSW |
2 |
155,263,651 (GRCm39) |
small deletion |
probably benign |
|
RF040:Ncoa6
|
UTSW |
2 |
155,263,651 (GRCm39) |
small deletion |
probably benign |
|
RF048:Ncoa6
|
UTSW |
2 |
155,263,632 (GRCm39) |
small deletion |
probably benign |
|
X0017:Ncoa6
|
UTSW |
2 |
155,248,460 (GRCm39) |
missense |
probably benign |
0.05 |
Z1176:Ncoa6
|
UTSW |
2 |
155,263,222 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ncoa6
|
UTSW |
2 |
155,263,138 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ncoa6
|
UTSW |
2 |
155,248,062 (GRCm39) |
missense |
possibly damaging |
0.67 |
|